RS587776446 HTRA1
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=255
Associated Conditions
CARASIL syndrome
HTRA1-related cerebral small vessel disease
Cerebral arteriopathy
autosomal dominant
with subcortical infarcts and leukoencephalopathy
type 2
CARASIL syndrome
HTRA1-related cerebral small vessel disease
Cerebral arteriopathy
autosomal dominant
with subcortical infarcts and leukoencephalopathy
type 2
Other Variants in HTRA1